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Clean and Clear Advantage

Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Clean & Clear Advantage Popped Pimple Relief Gel Pen


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active Ingredients

Salicylic Acid (2%)

Purpose

Acne medication Gel

Uses

  • For the management of acne

Warnings

For external use only.

When using this product

  • Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
  • Rinse right away with water if it gets in eyes.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Caution

Flammable. Do not use near fire, heat or while smoking.

Directions

  • Clean the skin thoroughly before applying this product.
  • Cover the entire affected area with a thin layer one to three times daily.
  • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
  • If bothersome dryness or peeling occurs, reduce application to once a day or every other day

Other Information

Dermatologists do not recommend intentionally popping pimples.

Inactive Ingredients

Water, SD Alcohol 40-B, Polyquaternium-37, Menthyl Lactate, C12-15 Alkyl Lactate, Potassium Lactate, Glycerin, Tetrahydroxypropyl Ethylenediamine, Chitosan PCA, Cetyl Lactate, Polysorbate 20, Cocamidopropyl PG-Dimonium Chloride Phosphate, Butylene Glycol, Fragrance, Benzalkonium Chloride, BHT, Portulaca Oleracea Extract, Citric Acid

PRINCIPAL DISPLAY PANEL - 1.7 g Carton

NEW
Clean
&
Clear®

advantage®
popped
pimple relief™
gel pen
salicylic acid acne medication

ON-THE-GO

designed to:
soothe soreness
clear up acne pimples
create a clear film

Net Wt. 0.06 Oz. (1.7 g)

Clean and Clear Advantage

Clean and Clear Advantage

Salicylic Acid GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:58232-0033
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Salicylic Acid SALICYLIC ACID 20 mg

Inactive Ingredients

Ingredient Name Strength
water
POTASSIUM LACTATE
POLYSORBATE 20
GLYCERIN
Edetol
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
BUTYLENE GLYCOL
benzalkonium chloride
BUTYLATED HYDROXYTOLUENE
CITRIC ACID MONOHYDRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1.7 in 1 CARTRIDGE
2 NDC:58232-0033-1 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partD part333D 2011-08-17


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Be sure to consult your doctor before taking any medication!
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